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Study on the damage caused by dimethyl phthalate on Pseudomonas fluorescens
Received:November 30, 2018  
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KeyWord:Dimethyl phthalate;Pseudomonas fluorescens;membrane damage;leakage of dissoluble matter
Author NameAffiliationE-mail
GUO Ru-xin College of Life Science and Agroforestry, Qiqihar University, Qiqihar 161006, China  
WANG Zhi-gang College of Life Science and Agroforestry, Qiqihar University, Qiqihar 161006, China wzg1980830@sina.com 
WANG Chun-long College of Life Science and Agroforestry, Qiqihar University, Qiqihar 161006, China  
YOU Yi-min College of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China  
WANG Heng-xu College of Life Science and Agroforestry, Qiqihar University, Qiqihar 161006, China  
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Abstract:
      Dimethyl phthalate(DMP)is a ubiquitous pollutant that is very harmful to microorganisms. Pseudomonas fluorescens(P. fluorescens)is one of the most important beneficial bacteria in the environment. To explore the toxicological effects of DMP on bacteria, P. fluorescens was selected and investigated using several bio-techniques, such as the polarization method, transmission electron microscopy, and ultra-high performance liquid chromatography. The results showed that the specific growth rate of P. fluorescens was slower, but the generation time was extended under the 10, 20 mg·L-1, and 40 mg·L-1 DMP treatments. The zeta potential on the surface of P. fluorescens decreased gradually from -12.21±0.56 mV to -18.13±0.67 mV under the 0, 10, 20 mg·L-1, and 40 mg·L-1 DMP treatments. Meanwhile, the mobility of the cell membrane increased by the DMP treatment and resulted in obvious cell deformation, severe plasmolysis, and leakage of dissoluble matter. The cumulative concentration of DMP inside the cells increased from 0.11±0.10 mg·L-1 to 6.78±0.25 mg·L-1, and the cumulative concentration outside the cells increased from 8.44±0.37 mg·L-1 to 30.52±0.88 mg·L-1, under the 10, 20 mg·L-1, and 40 mg·L-1 DMP treatments. Therefore, we conclude that DMP destroys the cell wall and the cell membrane of P. fluorescens and strongly affects the normal growth of P. fluorescens.